Allele Registry

Canonical Allele Identifier: PA122635

Gene: TG HGNC NCBI

ClinVar RCV:

RCV000013533

RCV000251808

RCV000277644

RCV001723563

RCV003716328

ClinVar Variation:

12696

2840391

HGVS (amino-acid)	Matching Registered Transcripts
NP_003226.4:p.Arg1999Trp	CA122634 NM_003235.5:c.5995C>T CA2739268970 NM_003235.5:c.5994_5995delinsGT